Ranitidine

Product NDC

63187-159

11-digit product format

631870159

Labeler code

63187

Product ID

63187-159_30086ccc-d5f8-45d8-90dd-a25d91289660

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA078542

Marketing category

ANDA

Marketing start

2008-11-19

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record